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NMR Studies of Drugs. Phensuximide. 1H and 13C NMR Methods with Chiral Solvating Agents and Lanthanide Shift Reagents
Authors:Robert Rothchild  Kerry Sanders  Kunisi S Venkatasubban
Institution:1. The City University of New York, John Jay College of Criminal Justice, Science Department, Toxicology Research and Training Center , 445 West 59th Street, New York, NY, 10019-1199;2. University of North Florida, Department of Natural Sciences , Jacksonville, FL, 32216
Abstract:NMR spectra of the racemic anticonvulsant, phensuximide, 1, in CDCl3 solution, have been studied with additives to explore methods for potential direct determination of enantiomeric excess (% ee). Proton studies at 200 MHz with the chiral solvating agent (CSA) (-)-2,2,2-trifluoro-1- (9-recommended for ee analysis due to uncertainties of contributions to the NCH3 from the CH2 proton absorptions.
Keywords:Optical purity  Enantiomeric excess  Analysis  Stereoisomers  LSR  CSA  Anticonvulsant  2  2  2-Trifluoro-1- (9-anthryl) ethanol  TFAE  Eu (FOD)3  Eu (HFC)3  Europium  1-Methyl-3-phenyl-2  5-pyrrolidinedione
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